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Association of inflammatory gene polymorphisms with mechanical heart valve reoperation

BACKGROUND: Various complications lead to reoperation in patients who undergo prosthetic valve replacement where inflammatory process could be involved. The goals of this study were to identify risk factors that correlate with reoperation in patients with prosthetic heart valves and to investigate t...

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Autores principales: Lee, Kyung Eun, Kim, Joo Hee, Chung, Jee Eun, Lee, Gwan Yung, Cho, Yoon Jeong, Chang, Byung Chul, Gwak, Hye Sun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929098/
https://www.ncbi.nlm.nih.gov/pubmed/27386381
http://dx.doi.org/10.1186/s40064-016-2566-x
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author Lee, Kyung Eun
Kim, Joo Hee
Chung, Jee Eun
Lee, Gwan Yung
Cho, Yoon Jeong
Chang, Byung Chul
Gwak, Hye Sun
author_facet Lee, Kyung Eun
Kim, Joo Hee
Chung, Jee Eun
Lee, Gwan Yung
Cho, Yoon Jeong
Chang, Byung Chul
Gwak, Hye Sun
author_sort Lee, Kyung Eun
collection PubMed
description BACKGROUND: Various complications lead to reoperation in patients who undergo prosthetic valve replacement where inflammatory process could be involved. The goals of this study were to identify risk factors that correlate with reoperation in patients with prosthetic heart valves and to investigate the relationship between reoperation and inflammatory gene polymorphisms. RESULTS: The study included 228 patients from the EwhA–Severance Treatment Group of Warfarin. Single nucleotide polymorphisms of c-reactive protein (CRP), interferon-gamma, interleukin 1 beta, interleukin 6, interleukin 10, transforming growth factor beta 1, and tumor necrosis factor genes were genotyped by means of SNaPshot and TaqMan assays. Thirty-nine patients (17.1 %) underwent more than one heart valve operation. A threefold increased risk for heart valve reoperation was evident in homozygous variant-type (TT) carriers as compared with ancestral allele carriers of CRP rs1205. Logistic regression analysis revealed that CRP rs1205 (OR 2.68, 95 % CI 1.22–5.90, p = 0.014), valve position (mitral valve OR 2.80, 95 % CI 1.01–7.80, p = 0.048; tricuspid valve OR 9.24, 95 % CI 2.46–34.70, p = 0.001; reference: aortic valve) and time after first operation (OR 1.13, 95 % CI 1.06–1.20, p < 0.001) affected the risk of reoperation. CONCLUSIONS: Inflammatory gene polymorphisms could be a possible marker of risk for reoperation in patients with prosthetic heart valve surgery.
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spelling pubmed-49290982016-07-06 Association of inflammatory gene polymorphisms with mechanical heart valve reoperation Lee, Kyung Eun Kim, Joo Hee Chung, Jee Eun Lee, Gwan Yung Cho, Yoon Jeong Chang, Byung Chul Gwak, Hye Sun Springerplus Research BACKGROUND: Various complications lead to reoperation in patients who undergo prosthetic valve replacement where inflammatory process could be involved. The goals of this study were to identify risk factors that correlate with reoperation in patients with prosthetic heart valves and to investigate the relationship between reoperation and inflammatory gene polymorphisms. RESULTS: The study included 228 patients from the EwhA–Severance Treatment Group of Warfarin. Single nucleotide polymorphisms of c-reactive protein (CRP), interferon-gamma, interleukin 1 beta, interleukin 6, interleukin 10, transforming growth factor beta 1, and tumor necrosis factor genes were genotyped by means of SNaPshot and TaqMan assays. Thirty-nine patients (17.1 %) underwent more than one heart valve operation. A threefold increased risk for heart valve reoperation was evident in homozygous variant-type (TT) carriers as compared with ancestral allele carriers of CRP rs1205. Logistic regression analysis revealed that CRP rs1205 (OR 2.68, 95 % CI 1.22–5.90, p = 0.014), valve position (mitral valve OR 2.80, 95 % CI 1.01–7.80, p = 0.048; tricuspid valve OR 9.24, 95 % CI 2.46–34.70, p = 0.001; reference: aortic valve) and time after first operation (OR 1.13, 95 % CI 1.06–1.20, p < 0.001) affected the risk of reoperation. CONCLUSIONS: Inflammatory gene polymorphisms could be a possible marker of risk for reoperation in patients with prosthetic heart valve surgery. Springer International Publishing 2016-06-30 /pmc/articles/PMC4929098/ /pubmed/27386381 http://dx.doi.org/10.1186/s40064-016-2566-x Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research
Lee, Kyung Eun
Kim, Joo Hee
Chung, Jee Eun
Lee, Gwan Yung
Cho, Yoon Jeong
Chang, Byung Chul
Gwak, Hye Sun
Association of inflammatory gene polymorphisms with mechanical heart valve reoperation
title Association of inflammatory gene polymorphisms with mechanical heart valve reoperation
title_full Association of inflammatory gene polymorphisms with mechanical heart valve reoperation
title_fullStr Association of inflammatory gene polymorphisms with mechanical heart valve reoperation
title_full_unstemmed Association of inflammatory gene polymorphisms with mechanical heart valve reoperation
title_short Association of inflammatory gene polymorphisms with mechanical heart valve reoperation
title_sort association of inflammatory gene polymorphisms with mechanical heart valve reoperation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929098/
https://www.ncbi.nlm.nih.gov/pubmed/27386381
http://dx.doi.org/10.1186/s40064-016-2566-x
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